Interesting facts
Interesting Facts about (2-isopropyl-5-methyl-phenyl) N-methylcarbamate
(2-isopropyl-5-methyl-phenyl) N-methylcarbamate is a fascinating compound with several notable properties and applications.
1. Chemical Structure and Functionality
- Carbamate Group: This compound features a carbamate functional group, which is known for its versatility and reactivity in organic synthesis.
- Isopropyl Substitution: The presence of the isopropyl and methyl substituents introduces steric effects that can greatly influence the compound's behavior in various chemical reactions.
2. Applications in Agriculture
This compound has been studied for its potential use as a pesticide. Its structure allows for:
- Pest Control: The specific arrangement of atoms makes it effective against certain pests, providing the agricultural sector with a safe and efficient alternative.
- Development of Safer Products: As chemical regulations become more stringent, compounds like this one are explored for creating less toxic pesticides.
3. Biological Insights
Research into the biological effects of (2-isopropyl-5-methyl-phenyl) N-methylcarbamate has revealed some intriguing aspects:
- Enzyme Inhibition: Similar carbamate derivatives have been shown to inhibit certain enzymes, which suggests potential applications in pharmacology.
- Safety Profile: Ongoing studies are assessing the safety and environmental impact of carbamate-containing compounds, emphasizing the importance of sustainability in chemical research.
4. Synthetic Routes
The synthesis of (2-isopropyl-5-methyl-phenyl) N-methylcarbamate is an interesting topic in organic chemistry, involving:
- Reagent Selection: Careful choice of reagents can lead to high yields and purity of the final compound.
- Reaction Conditions: Optimizing temperature and time can affect the overall efficiency of the reaction.
In summary, (2-isopropyl-5-methyl-phenyl) N-methylcarbamate exemplifies the blend of utility and complexity in modern chemistry. With its promising applications in agriculture and insights into biological interactions, it is a compound worth exploring further.
Synonyms
Thymol N-methylcarbamate
Thymol methylcarbamate
Methylcarbamic acid thymyl ester
3942-71-0
Methylcarbamic acid, thymol ester
CARBAMIC ACID, METHYL-, THYMYL ESTER
BRN 2330994
5-Methyl-2-(1-methylethyl)phenol methylcarbamate
Phenol, 5-methyl-2-(1-methylethyl)-, methylcarbamate
DTXSID00192595
4-06-00-03338 (Beilstein Handbook Reference)
DTXCID40115086
Phenol, 5-methyl-2-(1-methylethyl)-, methylcarbamate (9CI)
SCHEMBL11798229
(5-Methyl-2-propan-2-ylphenyl)n-methylcarbamate
Solubility of (2-isopropyl-5-methyl-phenyl) N-methylcarbamate
The solubility of the compound (2-isopropyl-5-methyl-phenyl) N-methylcarbamate can be influenced by multiple factors such as temperature, solvent type, and molecular structure. Generally, carbamates exhibit diverse solubility characteristics depending on their specific substituents.
Key points about its solubility include:
In conclusion, while (2-isopropyl-5-methyl-phenyl) N-methylcarbamate might demonstrate limited solubility in water, its behavior in organic solvents could showcase higher affinity, making it suitable for various applications in chemical formulations.